Quality Engineer III

Global healthcare company focused on innovative therapies, designing and manufacturing novel products for challenging medical conditions.
Alameda, CA, USA
$109,000 - $152,000
Quality
Mid-Level Software Engineer
In-Person
1,000 - 5,000 Employees
3+ years of experience
Healthcare · Biotech

Description For Quality Engineer III

Penumbra, Inc. is a leading global healthcare company based in Alameda, California, specializing in innovative medical devices and therapies. They're seeking a Quality Engineer III to join their team in developing life-saving medical devices. This role offers an exciting opportunity to work on high-impact projects ensuring the quality of interventional medical devices.

The position involves working with advanced scope problems, analyzing situations, and implementing quality objectives. You'll be responsible for leading development and qualification activities, designing QC processes, and supporting various quality-related initiatives. The role requires collaboration with multiple departments and suppliers while providing guidance to junior engineers.

The company offers a comprehensive benefits package including medical, dental, vision insurance, 401(k) with employer match, and stock purchase options. The work environment is collaborative and focused on continuous learning, with the opportunity to make a real impact in treating devastating diseases.

Ideal candidates should have 3+ years of quality engineering experience in medical devices, strong communication skills, and familiarity with quality systems regulations. The role offers competitive compensation ranging from $109,000 to $152,000 annually, reflecting the position's importance and responsibilities.

Working at Penumbra means joining a team that's revolutionizing medical treatments while maintaining the highest quality standards. The role combines technical expertise with leadership opportunities, making it perfect for quality professionals looking to advance their careers in the medical device industry.

Last updated 3 days ago

Responsibilities For Quality Engineer III

  • Collaborate and lead in development and qualification activities for new and existing products
  • Develop testing and inspection methodology and documentation
  • Lead Quality Objective teams
  • Design and install QC process sampling systems, procedures, and statistical techniques
  • Support activities like Inspections, NCRs, CAPAs, Engineering Change Orders
  • Perform failure analyses and defect investigations
  • Execute Continuous Improvement efforts
  • Support supplier activities and qualifications
  • Interface with other engineering departments and suppliers on quality issues
  • Provide guidance to junior Quality Engineers
  • Ensure compliance with QMS, regulations, standards, and procedures

Requirements For Quality Engineer III

  • Associate's or Bachelor's degree in Engineering, Life Science or related field
  • 3+ years of quality engineering or relevant experience in medical devices
  • Familiarity with QSR, ISO, and other applicable regulations
  • Excellent verbal, written, and interpersonal communication skills
  • Leadership skills
  • Proficiency with MS Word, Excel, and PowerPoint
  • Ability to lift and move up to 25 pounds
  • Vision abilities including close vision, distance vision, color vision

Benefits For Quality Engineer III

Medical Insurance
Dental Insurance
Vision Insurance
401k
Parental Leave
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • AD&D insurance
  • Short and long-term disability insurance
  • 401(k) with employer match
  • Employee stock purchase plan
  • Paid parental leave
  • 11 paid company holidays per year
  • 15 days minimum accrued vacation
  • Paid sick time

Interested in this job?

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